The FDA 's classification of the Queen Bee Gardens recall as Class II signals a moderate health risk, indicating that use or exposure to the affected products may cause temporary or medically reversible adverse health consequences, while the probability of serious adverse health consequences is remote.

More than 32 tons of butter have been recalled across the U.S. and in the Dominican Republic due to an undeclared allergen. Bunge North America issued a voluntary recall for 1,800 cases of butter on July 14 according to the FDA and that recall was given a Class 2 risk level where any use of or exposure to the product can “cause adverse health consequences.

The U.S. Food and Drug Administration (FDA) has elevated the risk classification for a nationwide butter recall, now labeling it a Class II recall — the second-highest warning level —due to a potential undeclared allergen.